EP2265616B8 - Furo-and thieno[3,2-c]pyridines - Google Patents

Furo-and thieno[3,2-c]pyridines Download PDF

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Publication number
EP2265616B8
EP2265616B8 EP09709265.4A EP09709265A EP2265616B8 EP 2265616 B8 EP2265616 B8 EP 2265616B8 EP 09709265 A EP09709265 A EP 09709265A EP 2265616 B8 EP2265616 B8 EP 2265616B8
Authority
EP
European Patent Office
Prior art keywords
furo
thieno
pyridines
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP09709265.4A
Other languages
German (de)
French (fr)
Other versions
EP2265616B1 (en
EP2265616A1 (en
Inventor
Mark J. Mulvihill
Jing Wang
Xin Chen
Ti Wang
An-Hu Li
Arno G. Steinig
Andrew Kleinberg
Qinghua Weng
Hanqing Dong
Meizhong Jin
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
OSI Pharmaceuticals LLC
Original Assignee
OSI Pharmaceuticals LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by OSI Pharmaceuticals LLC filed Critical OSI Pharmaceuticals LLC
Publication of EP2265616A1 publication Critical patent/EP2265616A1/en
Publication of EP2265616B1 publication Critical patent/EP2265616B1/en
Application granted granted Critical
Publication of EP2265616B8 publication Critical patent/EP2265616B8/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems
    • C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
EP09709265.4A 2008-02-06 2009-02-06 Furo-and thieno[3,2-c]pyridines Active EP2265616B8 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US6380008P 2008-02-06 2008-02-06
US11955308P 2008-12-03 2008-12-03
PCT/US2009/033311 WO2009100282A1 (en) 2008-02-06 2009-02-06 Furo-and thieno[3,2-c] pyridines

Publications (3)

Publication Number Publication Date
EP2265616A1 EP2265616A1 (en) 2010-12-29
EP2265616B1 EP2265616B1 (en) 2013-11-20
EP2265616B8 true EP2265616B8 (en) 2014-01-08

Family

ID=40524808

Family Applications (1)

Application Number Title Priority Date Filing Date
EP09709265.4A Active EP2265616B8 (en) 2008-02-06 2009-02-06 Furo-and thieno[3,2-c]pyridines

Country Status (19)

Country Link
US (1) US8022206B2 (en)
EP (1) EP2265616B8 (en)
JP (1) JP2011511094A (en)
KR (1) KR20110014971A (en)
CN (1) CN102007127A (en)
AR (1) AR070317A1 (en)
AU (1) AU2009212338A1 (en)
BR (1) BRPI0908050A2 (en)
CA (1) CA2711078A1 (en)
CL (1) CL2009000275A1 (en)
EA (1) EA201070929A1 (en)
ES (1) ES2451024T3 (en)
IL (1) IL206758A0 (en)
MX (1) MX2010008638A (en)
PE (1) PE20091414A1 (en)
TW (1) TW200944201A (en)
UY (1) UY31638A1 (en)
WO (1) WO2009100282A1 (en)
ZA (1) ZA201005554B (en)

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JP2013519681A (en) * 2010-02-11 2013-05-30 オーエスアイ・ファーマシューティカルズ，エルエルシー 7-aminofuropyridine derivative
US20120329826A1 (en) 2010-03-03 2012-12-27 OSI Pharmaceuticals,. LLC Substituted-5-aminopyrrolo/pyrazolopyridines
US8916593B2 (en) * 2010-05-04 2014-12-23 Pfizer Inc. Alkoxy-substituted 2-aminopyridines as ALK inhibitors
JP2013532627A (en) 2010-07-01 2013-08-19 武田薬品工業株式会社 Combination of cMET inhibitor with antibody against HGF and / or cMET
TWI504350B (en) * 2010-09-01 2015-10-21 Du Pont Fungicidal pyrazoles and their mixtures
US10614666B2 (en) 2011-04-20 2020-04-07 Video Gaming Technologies, Inc. Gaming machines with free play bonus mode presenting only winning outcomes
JP6118808B2 (en) 2011-10-31 2017-04-19 ザ メソジスト ホスピタル リサーチ インスティテュート Compounds comprising a MAO targeting / search moiety for treating human glioma
AU2013235487B2 (en) * 2012-03-23 2017-09-07 Memorial Sloan-Kettering Cancer Center Treatment of pancreatic and related cancers with 5-acyl-6,7-dihydrothieno[3,2-c]pyridines
WO2013152252A1 (en) 2012-04-06 2013-10-10 OSI Pharmaceuticals, LLC Combination anti-cancer therapy
KR101582852B1 (en) 2012-05-24 2016-01-07 서울대학교 산학협력단 Therapeutics for the treatment of neurodegenerative diseases mediated by Tau proteins
EP3483167A1 (en) 2013-06-26 2019-05-15 AbbVie Inc. Primary carboxamides as btk inhibitors
US9907791B2 (en) * 2014-03-14 2018-03-06 University Of Utah Research Foundation Ron inhibitors for use in preventing and treating bone loss
CN103923081B (en) * 2014-04-14 2017-06-27 武汉光谷人福生物医药有限公司 Compound and its preparation method and application
EP3229836B1 (en) 2014-12-09 2019-11-13 Institut National de la Sante et de la Recherche Medicale (INSERM) Human monoclonal antibodies against axl
WO2016135041A1 (en) 2015-02-26 2016-09-01 INSERM (Institut National de la Santé et de la Recherche Médicale) Fusion proteins and antibodies comprising thereof for promoting apoptosis
CN106866447A (en) * 2017-03-30 2017-06-20 成都绿林科技有限公司 A kind of method synthesized to acetylbenzene formamide
US10957159B2 (en) 2018-04-12 2021-03-23 Aristocrat Technologies Australia Pty Limited Gaming machine and method for displaying a free spin count-up
US11427596B2 (en) * 2019-07-19 2022-08-30 Indian Institute of Technology Indore Metal-free solvent-free synthesis of fused-pyrido heterocycles and biomedical applications
UY39890A (en) * 2021-08-10 2023-03-31 Jacobio Pharmaceuticals Co Ltd P53 MUTANT TARGET COMPOUNDS
EP4600246A4 (en) 2022-10-03 2026-01-07 Public Univ Corp Yokohama City Univ IMIDAZOPYRID INDERIVATES WITH BICYCLE STRUCTURE
AU2022488976A1 (en) * 2022-12-15 2025-06-12 Iregene Therapeutics Co., Ltd Inducer for inducing mesenchymal-epithelial transition and reprogramming

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US20040235867A1 (en) * 2001-07-24 2004-11-25 Bilodeau Mark T. Tyrosine kinase inhibitors
JP4505228B2 (en) * 2002-01-10 2010-07-21 バイエル・シェーリング・ファルマ・アクチェンゲゼルシャフト Rho-kinase inhibitor
US7704995B2 (en) * 2002-05-03 2010-04-27 Exelixis, Inc. Protein kinase modulators and methods of use
CL2003002287A1 (en) * 2002-11-25 2005-01-14 Wyeth Corp COMPOUNDS DERIVED FROM TIENO [3,2-b] -PIRIDINA-6-CARBONITRILOS AND TIENEO [2,3-b] -PIRIDINA-5-CARBONITRILS, PHARMACEUTICAL COMPOSITION, PROCEDURE OF PREPARATION AND INTERMEDIARY COMPOUNDS, AND THEIR USE IN THE TREATMENT OF CANCER, APOPLEJIA, OSTEOPOROSIS
US7276519B2 (en) * 2002-11-25 2007-10-02 Wyeth Thieno[3,2-b]pyridine-6-carbonitriles and thieno[2,3-b]pyridine-5-carbonitriles as protein kinase inhibitors
US7329678B2 (en) 2003-01-28 2008-02-12 Smithkline Beecham Corporation Chemical compounds
RS53118B (en) * 2003-02-26 2014-06-30 Sugen Inc. AMINOHETEROARYL UNITS AS PROTEIN KINASE INHIBITORS
EP1620094A4 (en) * 2003-05-06 2010-04-28 Glaxosmithkline Llc Novel chemical compounds
US20050026944A1 (en) * 2003-07-24 2005-02-03 Patrick Betschmann Thienopyridine and furopyridine kinase inhibitors
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US7601716B2 (en) * 2006-05-01 2009-10-13 Cephalon, Inc. Pyridopyrazines and derivatives thereof as ALK and c-Met inhibitors
PE20081581A1 (en) * 2006-12-21 2008-11-12 Plexxikon Inc PIRROLO [2,3-b] PYRIDINES COMPOUNDS AS KINASE MODULATORS
WO2008080015A2 (en) * 2006-12-21 2008-07-03 Plexxikon, Inc. Compounds and methods for kinase modulation, and indications therefor
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JP2011500778A (en) * 2007-10-25 2011-01-06 アストラゼネカ・アクチエボラーグ Pyridine and pyrazine derivatives-083
AR069393A1 (en) 2007-11-21 2010-01-20 Imclone Systems Inc INHIBITION OF THE RECEIVER FOR MACROFAGO STIMULATING PROTEIN (RON) AND METHODS FOR THE TREATMENT OF THE SAME
AU2009246263B2 (en) 2008-05-14 2014-08-21 Amgen Inc. Combinations VEGF(R) inhibitors and hepatocyte growth factor (c-Met) inhibitors for the treatment of cancer
KR101034351B1 (en) 2008-05-14 2011-05-16 한국화학연구원 Pyridine derivatives or pharmaceutically acceptable salts thereof substituted with novel benzoxazoles, preparation methods thereof, and pharmaceutical compositions for the prevention and treatment of abnormal cell growth diseases containing the same as active ingredients

Also Published As

Publication number Publication date
EP2265616B1 (en) 2013-11-20
EA201070929A1 (en) 2011-04-29
ES2451024T3 (en) 2014-03-26
UY31638A1 (en) 2009-09-30
CN102007127A (en) 2011-04-06
JP2011511094A (en) 2011-04-07
CA2711078A1 (en) 2009-08-13
MX2010008638A (en) 2010-08-30
WO2009100282A1 (en) 2009-08-13
BRPI0908050A2 (en) 2015-08-11
US8022206B2 (en) 2011-09-20
CL2009000275A1 (en) 2009-06-12
AU2009212338A1 (en) 2009-08-13
IL206758A0 (en) 2010-12-30
PE20091414A1 (en) 2009-09-23
ZA201005554B (en) 2011-04-28
KR20110014971A (en) 2011-02-14
EP2265616A1 (en) 2010-12-29
US20090197864A1 (en) 2009-08-06
TW200944201A (en) 2009-11-01
AR070317A1 (en) 2010-03-31

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